Canonical Allele Identifier: CA2586003637
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003821_47003822insGTA , CM000681.2:g.47003821_47003822insGTA GRCh38
NC_000019.9:g.47507078_47507079insGTA , CM000681.1:g.47507078_47507079insGTA GRCh37
NC_000019.8:g.52198918_52198919insGTA NCBI36
NG_047014.1:g.90255_90256insGTA
NG_047014.2:g.147825_147826insGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7633_7634insGTA ENSP00000385720.2:n.7633_7634insGTA
ENST00000672722.1:c.*3133_*3134insGTA MANE Select ENSP00000500409.1:n.*3133_*3134insGTA
ENST00000404338.7:c.7633_7634insGTA ENSP00000385720.2:n.7633_7634insGTA
ENST00000614079.1:c.7210_7211insGTA ENSP00000483730.1:n.7210_7211insGTA
NM_004491.4:c.7633_7634insGTA NP_004482.4:n.7633_7634insGTA
NM_004491.5:c.*3133_*3134insGTA MANE Select NP_004482.4:n.*3133_*3134insGTA